반응 #1888617

ord-512291c925104378b51b583b2db7fae5

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.DISSOLUTIONdissolved in a 2 L three-necked flask
  2. 2
    기타equipped with a thermometer
  3. 3
    온도while cooling in an ice bath
  4. 4
    기타was elevated to room temperature
  5. 5
    workup.ADDITIONwas added
  6. 6
    세척by washing with 200 mL of distilled water 5 times
  7. 7
    추출Thereafter, the extraction liquid
  8. 8
    농축was concentrated

실험 절차

165 g (584 mmol) of 2-(2-(2-methyl-2-adamantyloxy)-2-oxoethoxy)-2-oxoethanol, 2,000 mL, of tetrahydrofuran (THF), 105 mL (754 mmol) of triethylamine, and 0.165 g (1,000 ppm) of p-methoxyphenol were added to and dissolved in a 2 L three-necked flask equipped with a thermometer, a cooling pipe, and a stirrer. Then, 62.7 mL (648 mmol) of methacryloyl chloride was gradually added thereto while cooling in an ice bath. The temperature of the resultant was elevated to room temperature, and the resultant was stirred for 3 hours. Following completion of the reaction, 1,000 mL of diethyl ether was added thereto, followed by washing with 200 mL of distilled water 5 times. Thereafter, the extraction liquid was concentrated, thereby obtaining 198 g of an objective compound in the form of a colorless liquid (yield: 97%, GC purity: 99%).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08349534B2uspto-grants-2013_01